Fenwick M, Roizman B
J Virol. 1977 Jun;22(3):720-5. doi: 10.1128/JVI.22.3.720-725.1977.
Cells were enucleated with cytochalasin B after infection with herpes simplex virus 1. When protein synthesis was blocked by cycloheximide from the time of infection, mRNA for viral alpha-infected cell polypeptides (ICP) 4, 0, and 27 accumulated in the cytoplasm and was expressed after the removal of both drug and nucleus. A host protein, ICP 22, whose synthesis is stimulated in intact cells, was not made, and viral protein ICP4, which is normally modified to a form that migrates more slowly in polyacrylamide gels, was not modified in the absence of the nucleus. After enucleation at 2 h postinfection, a number of viral beta and gamma proteins continued to be made, starting at 20 to 25% of the normal rates and declining with a half-time of about 2 h. The synthesis of ICP 4 declined more rapidly, suggesting that it is switched off in the cytoplasm.
用单纯疱疹病毒1感染细胞后,用细胞松弛素B将细胞核去除。从感染时起用环己酰亚胺阻断蛋白质合成后,病毒α感染细胞多肽(ICP)4、0和27的mRNA在细胞质中积累,并在去除药物和细胞核后表达。一种宿主蛋白ICP 22,其合成在完整细胞中受到刺激,但在去核细胞中不产生,并且病毒蛋白ICP4,其通常被修饰为在聚丙烯酰胺凝胶中迁移较慢的形式,在没有细胞核的情况下不被修饰。在感染后2小时去核后,一些病毒β和γ蛋白继续产生,起始速率为正常速率的20%至25%,并以约2小时的半衰期下降。ICP 4的合成下降得更快,表明它在细胞质中被关闭。